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Hiring Company | アストラゼネカ株式会社 |
Location | Tokyo - 23 Wards |
Job Type | Permanent Full-time |
Salary | 6 million yen ~ 10 million yen |
【求人No NJB2258288】
■ 職務内容 / Job Description
Responsible for leading and managing clinical delivery team of contributing experts to operationally deliver defined clinical studies or clinical project work package / activities to time cost and appropriate quality in Japan R D.
Clinical Operations is the organisational home for the operational delivery and programme and project management of clinical projects drug and non drug.
Minimum Experience Level | No experience |
Career Level | Mid Career |
Minimum English Level | Business Level |
Minimum Japanese Level | Native |
Minimum Education Level | Bachelor's Degree |
Visa Status | Permission to work in Japan required |
■ 応募資格(経験、資格等)/ Qualification (Experience Skill etc.)
【経験 / Experience】
<必須 / Mandatory>
・At least 5 years’ experience from within the pharmaceutical industry or similar organization or academic experience.
・Extensive knowledge of clinical operations project management tools and processes
・Understanding of the skills and knowledge required for the successful delivery of a clinical study e.g. ICH GCP/J GCP local regulations study management
・Good experience of clinical development / drug development process in various phases of development and therapy areas
<歓迎 / Nice to have>
・Project management certification
・Working experiences in Clinical Development/ Quality Assurance
・PMDA GCP inspection
【資格 / License】
<必須 / Mandatory>
Bachelor’s Degree in Science or related discipline
<歓迎 / Nice to have>
Medical or biological sciences or discipline associated with clinical research.
【能力 / Skill set】
<必須 / Mandatory>
・Excellent Communication and relationship building skills
・Proven ability to prioritize and manage multiple tasks with conflicting deadlines
・Excellent interpersonal skills and proven ability to facilitate team building and team work
・Proactively identifies risks and issues and possible solutions
・Demonstrates ability to prepare and deliver study related training materials
・Demonstrates ability to plan coordinate and facilitate internal and external meetings
・Demonstrates professionalism and mutual respect
・Displays excellent organization and time management skills excellent attention to detail and ability to multi task in a high volume environment with shifting priorities
・Basic knowledge and experience of quality management
<歓迎 / Nice to have>
・Ability to interact widely and effectively within the company at all levels. Good networking skills
・Knowledge of process improvement methodology such as Lean Sigma/Change Management
・In depth knowledge of clinical and drug development process
・Fiscal and financial awareness
【語学 / Language】
<必須 / Mandatory>
英語 English: Business English (Achieve common understanding at the context level with customers)
Job Type | Permanent Full-time |
Salary | 6 million yen ~ 10 million yen |
Work Hours | 09:00 ~ 17:15 |
Holidays | 【有給休暇】有給休暇は入社時から付与されます 入社7ヶ月目には最低10日以上 【休日】完全週休二日制 年末年始 【有給休暇】※… |
Industry | Pharmaceutical |
Company Type | International Company |